rs1060502640

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs1060502640(-;-)

Make rs1060502640(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

32287614

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs1060502640
dbSNP (classic)	rs1060502640
ClinGen	rs1060502640
ebi	rs1060502640
HLI	rs1060502640
Exac	rs1060502640
Gnomad	rs1060502640
Varsome	rs1060502640
LitVar	rs1060502640
Map	rs1060502640
PheGenI	rs1060502640
Biobank	rs1060502640
1000 genomes	rs1060502640
hgdp	rs1060502640
ensembl	rs1060502640
geneview	rs1060502640
scholar	rs1060502640
google	rs1060502640
pharmgkb	rs1060502640
gwascentral	rs1060502640
openSNP	rs1060502640
23andMe	rs1060502640
SNPshot	rs1060502640
SNPdbe	rs1060502640
MSV3d	rs1060502640
GWAS Ctlg	rs1060502640

Max Magnitude

0

ClinVar
Risk	rs1060502640(-;-)
Alt	rs1060502640(-;-)
Reference	Rs1060502640(G;G)
Significance	Pathogenic
Disease	Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32305731delC
CLNSRC
CLNACC	RCV000466920.1,